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Potassium Chloride - 68084-632-01 - (Potassium Chloride)

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Drug Information of Potassium Chloride

Product NDC: 68084-632
Proprietary Name: Potassium Chloride
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 10    meq/1 & nbsp;   Potassium Chloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride

Product NDC: 68084-632
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075604
Marketing Category: ANDA
Start Marketing Date: 20130118

Package Information of Potassium Chloride

Package NDC: 68084-632-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-632-01) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-632-11)

NDC Information of Potassium Chloride

NDC Code 68084-632-01
Proprietary Name Potassium Chloride
Package Description 10 BLISTER PACK in 1 CARTON (68084-632-01) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-632-11)
Product NDC 68084-632
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130118
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name POTASSIUM CHLORIDE
Strength Number 10
Strength Unit meq/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride


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